Canonical Allele Identifier: CA2154909550

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1890108749

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279442_91279450del , CM000676.2:g.91279442_91279450del	GRCh38
NC_000014.8:g.91745786_91745794del , CM000676.1:g.91745786_91745794del	GRCh37
NC_000014.7:g.90815539_90815547del	NCBI36
NG_033118.1:g.143396_143404del
NG_033118.2:g.143396_143404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-143_4700-135del MANE Select	ENSP00000374507.6:n.4700-143_4700-135del
ENST00000331194.8:c.272-143_272-135del	ENSP00000330332.8:n.272-143_272-135del
ENST00000334448.5:n.512-143_512-135del
ENST00000389857.10:c.4700-143_4700-135del	ENSP00000374507.6:n.4700-143_4700-135del
ENST00000556726.5:c.928-143_928-135del
ENST00000557455.1:n.529_537del
NM_001080414.3:c.4700-143_4700-135del	NP_001073883.2:n.4700-143_4700-135del
XM_011536796.1:c.4592-143_4592-135del	XP_011535098.1:n.4592-143_4592-135del
XR_429316.2:n.4975-143_4975-135del
XR_943459.1:n.5440_5448del
XM_011536796.2:c.4592-143_4592-135del	XP_011535098.1:n.4592-143_4592-135del
XM_017021335.2:c.*431_*439del	XP_016876824.1:n.*431_*439del
XM_017021336.1:c.1781-143_1781-135del	XP_016876825.1:n.1781-143_1781-135del
XR_429316.4:n.4973-143_4973-135del
NM_001080414.4:c.4700-143_4700-135del MANE Select	NP_001073883.2:n.4700-143_4700-135del